Amyloid-targeting treatment in Alzheimer's disease and concomitant antiplatelets: a clinical gray zone? - Summary - MDSpire

Amyloid-targeting treatment in Alzheimer's disease and concomitant antiplatelets: a clinical gray zone?

  • By

  • Rus Prelog, Polona

  • Zupan, Matija

  • Kovacic, Alenka

  • Frol, Senta

  • Gregoric Kramberger, Milica

  • May 4, 2026

  • 0 min

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Objective:

To discuss the safety concerns of concomitant antiplatelet treatment in patients with Alzheimer's disease receiving amyloid-targeting therapies (ATTs), particularly focusing on the potential risk of amyloid-related imaging abnormalities (ARIAs) and their clinical implications.

Key Findings:
  • Approximately 2.2 million in the US and ~5.9 million in the EU may be eligible for ATT, with a significant proportion at risk for ARIA.
  • APOE ε4 carriers have a higher risk of ARIA, which can be exacerbated by certain comorbidities and medications, necessitating careful patient assessment.
  • Concomitant use of antiplatelet agents, especially dual antiplatelet therapy (DAPT), may increase the risk of ARIA-H in patients on ATTs, highlighting the need for caution.
  • SSRIs and NSAIDs are commonly prescribed in older adults and may pose additional bleeding risks, warranting further investigation.
Interpretation:

The intersection of amyloid-targeting therapies and antiplatelet use presents a complex clinical dilemma, necessitating careful consideration of patient selection and medication interactions to mitigate risks.

Limitations:
  • Lack of real-world data on the safety of ATTs in patients with concurrent antiplatelet therapy limits the ability to generalize findings to broader populations.
  • Exclusion of certain patient populations from RCTs, such as those with comorbidities or concurrent medications, limits the generalizability of findings and raises concerns about safety in diverse clinical settings.
Conclusion:

Further research is needed to clarify the safety of antiplatelet use in patients receiving amyloid-targeting therapies, particularly regarding the risk of ARIA and intracranial hemorrhage, to inform clinical practice and improve patient outcomes.

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